EP3013459A1 - Procede et dispositif de traitement de gaz par injection de compose pulverulent et de phase aqueuse - Google Patents
Procede et dispositif de traitement de gaz par injection de compose pulverulent et de phase aqueuseInfo
- Publication number
- EP3013459A1 EP3013459A1 EP14736324.6A EP14736324A EP3013459A1 EP 3013459 A1 EP3013459 A1 EP 3013459A1 EP 14736324 A EP14736324 A EP 14736324A EP 3013459 A1 EP3013459 A1 EP 3013459A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- compound
- aqueous phase
- injection
- powdery
- gases
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract description 175
- 239000008346 aqueous phase Substances 0.000 title claims abstract description 116
- 238000000034 method Methods 0.000 title claims abstract description 30
- 239000007789 gas Substances 0.000 claims abstract description 89
- 239000002245 particle Substances 0.000 claims abstract description 40
- 239000003344 environmental pollutant Substances 0.000 claims abstract description 18
- 231100000719 pollutant Toxicity 0.000 claims abstract description 18
- 238000002347 injection Methods 0.000 claims description 152
- 239000007924 injection Substances 0.000 claims description 152
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 69
- 235000010755 mineral Nutrition 0.000 claims description 69
- 239000011707 mineral Substances 0.000 claims description 69
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 54
- 239000000920 calcium hydroxide Substances 0.000 claims description 53
- 235000011116 calcium hydroxide Nutrition 0.000 claims description 53
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims description 51
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims description 51
- 239000000843 powder Substances 0.000 claims description 24
- 230000002093 peripheral effect Effects 0.000 claims description 18
- 230000008569 process Effects 0.000 claims description 11
- 239000002253 acid Substances 0.000 claims description 10
- 229910052799 carbon Inorganic materials 0.000 claims description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- 239000007864 aqueous solution Substances 0.000 claims description 6
- 239000012071 phase Substances 0.000 claims description 6
- 150000007513 acids Chemical class 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- 238000011084 recovery Methods 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 4
- 238000009413 insulation Methods 0.000 claims description 4
- 239000004113 Sepiolite Substances 0.000 claims description 3
- HPTYUNKZVDYXLP-UHFFFAOYSA-N aluminum;trihydroxy(trihydroxysilyloxy)silane;hydrate Chemical compound O.[Al].[Al].O[Si](O)(O)O[Si](O)(O)O HPTYUNKZVDYXLP-UHFFFAOYSA-N 0.000 claims description 3
- 239000000571 coke Substances 0.000 claims description 3
- 229910052621 halloysite Inorganic materials 0.000 claims description 3
- 239000003077 lignite Substances 0.000 claims description 3
- 229910052624 sepiolite Inorganic materials 0.000 claims description 3
- 235000019355 sepiolite Nutrition 0.000 claims description 3
- 229910021529 ammonia Inorganic materials 0.000 claims description 2
- 230000015572 biosynthetic process Effects 0.000 claims description 2
- 150000001722 carbon compounds Chemical class 0.000 claims description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 2
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 claims 1
- 150000004820 halides Chemical class 0.000 claims 1
- 235000017550 sodium carbonate Nutrition 0.000 claims 1
- 239000003546 flue gas Substances 0.000 description 75
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 52
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 41
- 235000011941 Tilia x europaea Nutrition 0.000 description 41
- 239000004571 lime Substances 0.000 description 41
- 150000002484 inorganic compounds Chemical class 0.000 description 15
- 229910010272 inorganic material Inorganic materials 0.000 description 15
- 239000007921 spray Substances 0.000 description 12
- 238000011144 upstream manufacturing Methods 0.000 description 10
- 238000001816 cooling Methods 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 8
- 238000011065 in-situ storage Methods 0.000 description 8
- 230000009467 reduction Effects 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 239000000725 suspension Substances 0.000 description 7
- 238000005054 agglomeration Methods 0.000 description 5
- 230000002776 aggregation Effects 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 4
- 239000002250 absorbent Substances 0.000 description 3
- 230000002745 absorbent Effects 0.000 description 3
- 229940125782 compound 2 Drugs 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- -1 for example Chemical compound 0.000 description 3
- 239000003517 fume Substances 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 150000002013 dioxins Chemical class 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 150000002240 furans Chemical class 0.000 description 2
- 229910001385 heavy metal Inorganic materials 0.000 description 2
- 239000004572 hydraulic lime Substances 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 239000008267 milk Substances 0.000 description 2
- 210000004080 milk Anatomy 0.000 description 2
- 235000013336 milk Nutrition 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000007790 solid phase Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- SZUVGFMDDVSKSI-WIFOCOSTSA-N (1s,2s,3s,5r)-1-(carboxymethyl)-3,5-bis[(4-phenoxyphenyl)methyl-propylcarbamoyl]cyclopentane-1,2-dicarboxylic acid Chemical compound O=C([C@@H]1[C@@H]([C@](CC(O)=O)([C@H](C(=O)N(CCC)CC=2C=CC(OC=3C=CC=CC=3)=CC=2)C1)C(O)=O)C(O)=O)N(CCC)CC(C=C1)=CC=C1OC1=CC=CC=C1 SZUVGFMDDVSKSI-WIFOCOSTSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 230000000712 assembly Effects 0.000 description 1
- 238000000429 assembly Methods 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 229940126543 compound 14 Drugs 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229910052615 phyllosilicate Inorganic materials 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000000306 recurrent effect Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M sodium bicarbonate Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 150000003388 sodium compounds Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
- B01D53/81—Solid phase processes
- B01D53/83—Solid phase processes with moving reactants
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/38—Removing components of undefined structure
- B01D53/40—Acidic components
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/46—Removing components of defined structure
- B01D53/48—Sulfur compounds
- B01D53/50—Sulfur oxides
- B01D53/501—Sulfur oxides by treating the gases with a solution or a suspension of an alkali or earth-alkali or ammonium compound
- B01D53/504—Sulfur oxides by treating the gases with a solution or a suspension of an alkali or earth-alkali or ammonium compound characterised by a specific device
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/74—General processes for purification of waste gases; Apparatus or devices specially adapted therefor
- B01D53/80—Semi-solid phase processes, i.e. by using slurries
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23J—REMOVAL OR TREATMENT OF COMBUSTION PRODUCTS OR COMBUSTION RESIDUES; FLUES
- F23J15/00—Arrangements of devices for treating smoke or fumes
- F23J15/003—Arrangements of devices for treating smoke or fumes for supplying chemicals to fumes, e.g. using injection devices
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23J—REMOVAL OR TREATMENT OF COMBUSTION PRODUCTS OR COMBUSTION RESIDUES; FLUES
- F23J7/00—Arrangement of devices for supplying chemicals to fire
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2251/00—Reactants
- B01D2251/30—Alkali metal compounds
- B01D2251/304—Alkali metal compounds of sodium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2251/00—Reactants
- B01D2251/40—Alkaline earth metal or magnesium compounds
- B01D2251/404—Alkaline earth metal or magnesium compounds of calcium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2251/00—Reactants
- B01D2251/60—Inorganic bases or salts
- B01D2251/602—Oxides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2251/00—Reactants
- B01D2251/60—Inorganic bases or salts
- B01D2251/606—Carbonates
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2253/00—Adsorbents used in seperation treatment of gases and vapours
- B01D2253/10—Inorganic adsorbents
- B01D2253/102—Carbon
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2253/00—Adsorbents used in seperation treatment of gases and vapours
- B01D2253/10—Inorganic adsorbents
- B01D2253/106—Silica or silicates
- B01D2253/11—Clays
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2257/00—Components to be removed
- B01D2257/20—Halogens or halogen compounds
- B01D2257/204—Inorganic halogen compounds
- B01D2257/2045—Hydrochloric acid
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2257/00—Components to be removed
- B01D2257/20—Halogens or halogen compounds
- B01D2257/204—Inorganic halogen compounds
- B01D2257/2047—Hydrofluoric acid
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2257/00—Components to be removed
- B01D2257/30—Sulfur compounds
- B01D2257/302—Sulfur oxides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2257/00—Components to be removed
- B01D2257/60—Heavy metals or heavy metal compounds
- B01D2257/602—Mercury or mercury compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2258/00—Sources of waste gases
- B01D2258/02—Other waste gases
- B01D2258/0283—Flue gases
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2259/00—Type of treatment
- B01D2259/12—Methods and means for introducing reactants
- B01D2259/126—Semi-solid reactants, e.g. slurries
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/02—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
- B01D53/06—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with moving adsorbents, e.g. rotating beds
- B01D53/10—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography with moving adsorbents, e.g. rotating beds with dispersed adsorbents
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23J—REMOVAL OR TREATMENT OF COMBUSTION PRODUCTS OR COMBUSTION RESIDUES; FLUES
- F23J2219/00—Treatment devices
- F23J2219/50—Sorption with semi-dry devices, e.g. with slurries
Definitions
- the present invention relates to a gas treatment method having a predetermined direction of flow in a gas line comprising the steps
- the treatment of gases requires the abatement of acid gases, especially HCl, S0 2 and / or HF, which abatement can be carried out dry, by injection of a substance, often mineral, dry and pulverulent in a stream of flue gas or through a filter comprising a fixed bed of solid particles or moving.
- the powdery compound generally comprises a calco-magnesium compound, in particular lime, preferably quenched or hydrated or a sodium compound such as sodium carbonate or bicarbonate.
- inorganic compounds may also be used, especially those used for the reduction of dioxins, furans and / or heavy metals, including mercury, such as, for example, those based on phyllosilicates, such as sepiolite or halloysite or the like.
- the present invention relates more particularly to processes for reducing acid gases in gases, in particular flue gases, by injecting a powdery product having capturing acidic pollutants in the gas stream to improve the abatement efficiencies of the gaseous acid components of the treated gases.
- Documents CN 2011 68568 and JP 10-216 572 each propose an alternative intended to solve clogging problems by carrying out the suspension of lime milk in situ during the injection.
- a lance consisting of two concentric tubes, that is to say an inner tube and an outer tube.
- the water is injected via the inner tube while the hydrated lime is injected via the outer tube.
- the position of the inner tube can be adjusted with respect to the position of the outer tube and it is therefore possible to have an inner tube for the water having an outlet port projecting or recessed or at the same level relative to a hydrated lime outlet port of the outer tube.
- the design of the spray lances requires the water spray tube to be internal to the pulverized hydrated lime spray tube.
- the sprayed lime encounters an obstacle within the outer spray tube that resides in the inner water spray tube.
- the moisture content of the hydrated lime induces a water / lime mass ratio of 5 to 6 to form a suspension in situ.
- This suspension provides an adverse side effect for the treatment of flue gas in that the gas is furthermore significantly cooled with the injection of hydrated lime. This assumes that the fumes are hot enough for the depollution to be effective; however, this is not sought after today as industrialists have an increasing tendency to recover the heat of the flue gas at best for economic and environmental reasons.
- the present invention aims to overcome the drawbacks of the state of the art by providing a process for the treatment of gases, in particular flue gas, with a powdery compound, preferably mineral, in particular hydrated lime, during which the risk of clogging is significantly reduced and the water consumption is minimized and without substantially cooling the gases, thus allowing not to interfere with the recovery of calories from these gases to be treated.
- gases in particular flue gas
- a powdery compound preferably mineral, in particular hydrated lime
- a method as indicated at the beginning characterized in that said step of injecting aqueous phase, in the form of droplets, is carried out inside said gas pipe in said cloud or flow of particles of powdery compound, so as to moisten these particles of powdery compound inside the gas line, during their injection, in a weighted ratio between the aqueous phase injected in the form of droplets and the injected powdery compound greater than or equal to 0.05 and less than or equal to 1.2.
- the humidification of the powdery compound is carried out at the point of injection of the powdery compound, and this in the conduit / gas stream to be treated.
- the particles of the inorganic compound and the water phase droplets coexist very locally, and the powdery compound is moistened in situ and in a controlled manner.
- a layer of droplets of aqueous phase is thus created on the surface of the particles of powdery compound and facilitates the transfer of pollutants, especially acids, to be slaughtered to the solid phase of the powdery compound.
- the aqueous phase droplet layer is obtained via the controlled co-injection of powdery compound and aqueous phase particles according to said weight ratio and the in situ wetting of the powdery compound avoids the recurrent problem of clogging the compound injection lances. powder, in particular hydrated hydrated lime.
- the aqueous phase is injected in an immediate vicinity with respect to the powder compound injection point.
- the term "immediate vicinity" means that the distance between the point of injection of the aqueous phase and the injection point of the powdery compound is less than or equal to the diameter of the injection point. the powder compound injection tubing, in particular less than or equal to the radius.
- the powdery compound is a mineral compound. It may comprise a calco-magnesium compound, in particular lime, preferably quenched or hydrated.
- the mineral compound is chosen from those used for the abatement of dioxins, furans and / or heavy metals including mercury, for example those based on sepiolite or halloysite or the like.
- the pulverulent compound used may also be organic, in particular carbon-based, in particular of the activated carbon or lignite coke type.
- the powdery compound can also be a mixture of these compounds.
- the aqueous phase is liquid water or an aqueous solution of alkaline compound selected from the group consisting of metal hydroxides, carbonates, bicarbonates, hydrogencarbonates, nitrates, phosphates, persulfates, and monocarboxylates.
- alkali especially sodium, potassium and / or lithium, and mixtures thereof, or an aqueous solution of ammonia or urea-based compound, such as ammonium salts, or an aqueous solution of compound with base of alkali or alkaline-earth metal or ammonium halides, in particular chloride and / or bromide, especially sodium, potassium, calcium or magnesium.
- the aqueous phase may also contain acids, especially organic acids, difunctional (di-basic acids) or not.
- the aqueous phase is essentially monophasic.
- the aqueous phase consists essentially of a liquid, in particular liquid water.
- the temperature of the aqueous phase before injection into said flue gas duct is less than 100 ° C, preferably less than 40 ° C, particularly less than 30 ° C, more particularly less than 20 ° C.
- the aqueous phase injection step is carried out in a neighborhood immediately downstream of said powder compound injection point with respect to said predetermined flow direction of the gases in said gas pipe.
- neighborhborhood immediately downstream of the injection point of powdery compound is meant in the sense of the present invention, that, with respect to the flow direction of the gases, the aqueous phase droplets are pulverized just after the compound powder.
- the injected powdery compound therefore first encounters the gases and immediately after the aqueous phase droplets formed, which thus makes it possible to moisten the powdery compound and not the gases to be treated.
- the aqueous phase injection step is carried out in a neighborhood immediately upstream of said mineral compound injection point with respect to said predetermined flow direction of the flue gases in said gas pipe. of fumes.
- said pulverulent compound injection step is carried out in the gas pipeline in an injection direction which forms an angle of 90 to 150 degrees, preferably less than or equal to 145 degrees, preferentially less than or equal to 40 degrees. degrees and in particular less than or equal to 135 degrees, with respect to the predetermined flow direction of the gases.
- said aqueous phase droplets have an average droplet size of between 500 and 5000 ⁇ m, preferably between 500 and 5000 ⁇ m, depending on the injection conditions.
- said powdery compound in particular powdered hydrated lime, has an average particle size d.sub.50 of less than 80 .mu.m, advantageously less than 50 .mu.m, preferably less than 35 .mu.m, preferably less than 25 .mu.m and in particular less than or equal to 10 ⁇ m, in particular less than or equal to 8 ⁇ m.
- the powdery compound may be a powdery inorganic compound co-injected with another pulverulent compound, especially a carbon compound, in particular of the activated carbon or lignite coke type.
- said pulverulent compound in particular hydrated lime, has a moisture (mass content of water) of between 0.2% and 10% before injection into said gas line. especially between 0.5 and 4%, preferably less than 2%, in particular less than 1.5%.
- the weight ratio between said aqueous phase injected in the form of droplets and said injected powdery compound is greater than or equal to 0.1, preferably greater than or equal to 0.2, and less or equal to 1, and more particularly less than or equal to 0.8.
- This weight ratio is relatively low in comparison with that reported in the previous documents CN 1 685 68 and JP 10-216 572 and does not cause any substantial cooling of the gases to be treated because, according to the present invention, the reduced proportion of water added allows the humidification of the powdery compound, in particular hydrated lime, without moistening and thus significantly cool the gases.
- the high weight ratio between water and hydrated lime of between 5 and 6 is dictated by the fact that a suspension of hydrated lime (milk of lime) is sprayed into the gas to be treated.
- the temperature of the gases is greatly reduced by the injection of a large quantity of water which consumes calories on evapo- ration.
- said gases have, before injection of said powdery compound, a temperature of between 10 and 1100.degree. in particular between 10 and 100 ° C, especially between 15 and 80 ° C, in particular between 20 and 70 ° C or between 100 ° C and 300 ° C, preferably between 30 ° C and 250 ° C and preferably between 150 and 150 ° C. C. and 230 ° C., in particular between 160 ° C. and 220 ° C.
- said gases have, before injection of said powdery compound, a temperature of between 300 ° C. and 500 ° C., preferably between 320 ° C. and 450 ° C., preferably between 330 ° C. and 400 ° C or between 850 and 1100 ° C, preferably between 900 and 1100 ° C and preferably between 950 ° C and 1050 ° C
- the temperature of the gases is not significantly influenced by the small amount of water and the size of the droplets which according to the invention contribute substantially to moisten the powdery compound.
- the aqueous phase injection taking place in the cloud of injected powdery compound especially in an immediate vicinity of the injection point of the powdery compound, the contact between the aqueous phase droplets and the particles of powdery compound is promoted and very fast, which allows an optimization of the reduction of acid pollutants, facilitated by the layer of water formed around the particles of powdery compound.
- said gases have, after injection of said powdery compound and of said aqueous phase in the form of droplets, a temperature of between n and n-10 ° C., preferably between n and n-8 °. C, preferably between n and n - 5 ° C, in particular between n and n - 3 ° C, n being the temperature of the gases before injection of the powdery compound and the aqueous phase.
- said injection of the aqueous phase is carried out through a spray pipe, preferably in the form of a fan plane jet, at a pressure of between 2 and 150 bar.
- this pressure will be between 2 and 20 bar, preferably between 3 and 15 bar and preferably about 8 bar.
- the pressure will be between 20 and 150 bar, in particular between 30 and 100 bar.
- the invention also relates to a device for injecting pulverulent compound, preferably mineral, in particular powdered hydrated lime, into a gas pipe comprising a powder compound injection tubing, connected to a source of powdery compound and arranged to open into said gas line, said powdery substance injection tubing having an outer face and an inner face arranged to be in contact with said powdery compound, said powdery compound injection device further comprising at least one tubing aqueous phase injection in the form of droplets connected to an aqueous phase source.
- pulverulent compound preferably mineral, in particular powdered hydrated lime
- Such a device is known from the state of the art, such as, for example, documents CN 1 68568 and JP 10-26 572.
- the water injection tubing is concentric to a larger hydrated lime injection tubing for hydrated lime slurry in situ.
- CN 2011 68568 it is provided in some flue gas treatment devices by a lime pit that the position of the inner tube can be adjusted with respect to the position of the outer tube.
- the inner tube for water has an outlet port projecting or recessed or at the same level with respect to a hydrated lime outlet port of the outer tube.
- the concentric configuration and the desire to form a suspension of hydrated lime in situ has the effect that a water / lime ratio of 5 to 6 is required.
- the device according to the documents CN 2011 68568 and JP 10-216 572 has the effect of cooling the flue gases, thus posing a new problem for industrial players increasingly having a tendency to recover the fumes. calories from flue gases to offer more economical and environmentally friendly processes.
- the present invention aims to overcome the drawbacks of the state of the art by providing a device for the injection of pulverulent compound, preferably mineral, in particular hydrated lime, and the humidification of its particles in the treatment of gas whose risk of clogging is significantly reduced, and this without cooling the gases, thus allowing not to interfere with the recovery of calories from these gases to be treated.
- pulverulent compound preferably mineral, in particular hydrated lime
- a device as indicated above characterized in that said at least one aqueous phase injection nozzle is located in a peripheral space located around said outer face of the tubing injection of powdery compound.
- said at least one aqueous phase tubing located in a peripheral space located around the outer face of the powder compound injection tubing is thus arranged to allow injection of droplets of aqueous phase, in particular liquid water. in an immediate vicinity with respect to the powder compound injection point.
- immediate vicinity is intended to mean that the distance separating the outside diameters of the aqueous phase and powder compound injection pipes respectively is less than or equal to the diameter of the powder compound injection tubing, preferably less than the radius.
- the particular configuration of said at least one aqueous phase injection pipe and said powder compound injection pipe makes it possible to treat the gases in quasi-dry manner, by only humidifying the powdery compound, in particular lime, and in the latter case, without forming a suspension of whitewash. This operation is carried out without significantly humidifying the gases, and thus without cooling the gases whose heat recovery is more and more desired.
- This particular configuration does not require, unlike the state of the art disclosed in CN 201 68568 and JP 10-216 572, weight ratio high water lime and reduces the value from between 5 and 6 to a value less than or equal to 1, 2 preferably less than or equal to 1, more particularly less than or equal to 0.8.
- a cloud of particles of powdery compound in particular of hydrated lime
- aqueous phase in particular water
- these droplets of aqueous phase meet the dense cloud of particles of powder compound and improve the abatement of pollutants, including acidic compounds of gases, without cooling the gases.
- the device comprises a plurality of aqueous phase injection tubes in the form of droplets, each connected to a distributor connected to said source of aqueous phase, each manifold of said plurality of injection manifolds being located in said peripheral space, each pipe being further provided with a valve.
- each aqueous phase injection tubing is arranged in a concentric tube, out of which the aqueous phase injection tubing is retractable.
- each aqueous phase injection tubing has an outlet port in the form of a slot or spray nozzle.
- the dispenser is connected to a pressurizing means arranged to give the aqueous phase a pressure of between 2 and 150 bar, in particular between 2 and 20 bar, preferably between 3 and 15 bar, and more preferably about 8 bar and in another variant between 20 and 150 bar, in particular between 30 and 100 bar.
- a pressurizing means arranged to give the aqueous phase a pressure of between 2 and 150 bar, in particular between 2 and 20 bar, preferably between 3 and 15 bar, and more preferably about 8 bar and in another variant between 20 and 150 bar, in particular between 30 and 100 bar.
- It can of course be a feed in the aqueous phase, in particular in liquid water, directly available at the aforementioned pressures.
- the device comprises an outer envelope around said peripheral space.
- the device according to the present invention comprises, in said peripheral space, at least one insulating layer between said outer face of said powder compound injection tubing and said outer casing.
- the device further comprises a device for closing said peripheral space provided with a series of orifices, among which a powder compound orifice and at least one aqueous phase orifice, said orifice composition with a powder compound being arranged to house an outlet of said powder compound injection tubing, each aqueous phase port being arranged to house an outlet of each aqueous phase injection tubing.
- said outer envelope has a diameter of between 100 and 250 mm, preferably less than 200 mm and more preferably between 0 and 170 mm, in particular between 25 and 150 mm.
- said powder compound injection tubing has a diameter of between 75 and 150 mm, preferably between 80 and 125 mm and in particular about 100 mm.
- each aqueous phase injection tubing has a diameter of between 5 and 30 mm, preferably between 6 and 20 mm and more preferably between 8 and 16 mm.
- FIG. 1A is a schematic side view of a first embodiment of the gas treatment apparatus according to the present invention.
- Figure 1B is a sectional view along the line 11 of Figure 1A.
- Fig. 2A is a schematic side view of a second embodiment of the gas treatment apparatus according to the present invention.
- Figure 2B is a sectional view along the line II-II of Figure 2A.
- FIG. 3 is a schematic side view of the embodiment according to FIG. 1 of the gas treatment device according to the present invention, used for example in a flue gas duct, the injection direction of the powdery compound being here perpendicular to the flow direction of the flue gases.
- FIG. 4 is a schematic side view of the second embodiment according to FIG. 2 of the flue gas treatment device according to the present invention, used in a flue gas duct, the injection direction of the powdery compound being here also perpendicular to the flow direction of the flue gases.
- Figure 5 is a schematic side view of the embodiment according to Figure 2 of the flue gas treatment device according to the present invention, used in a flue gas duct.
- the direction of injection of the powdery compound is located obliquely to the flow direction of the flue gas.
- Figures 3 to 5 illustrate modes, among others, of coupling devices according to the invention to a flue gas duct.
- the powdered compound injected is in the illustrated cases of mineral nature and the treated gases are flue gases.
- the device according to the present invention is a device for injecting pulverulent inorganic compound 1 to be introduced into a flue gas line, comprising a pulverulent inorganic compound injection pipe 2 connected to a source of pulverulent inorganic compound (not shown).
- the mineral compound injection tubing is arranged to open into said flue gas duct 3 (see FIG. 3) and to allow the exit of the inorganic compound via a mineral compound outlet port 14.
- the compound injection tubing mineral 2 has an outer face 4 and an inner face 5. In operation, the inner face 5 is in contact with said powdery mineral compound during its feeding into the injection pipe 2.
- the pulverulent inorganic compound injection device 1 comprises a plurality of aqueous phase injection tubes 6 in the form of droplets, each connected to a distributor 7 connected to an aqueous phase feed 8.
- each tubing 6 of the plurality of injection tubings is located around the mineral compound injection tubing 2 in a space outside thereof, referred to herein as the peripheral space 9.
- Each The aqueous phase injection tubing 6 further comprises a valve 0 situated between the distributor 7 and the aqueous phase outlet 1 of each aqueous phase injection tubing 6.
- aqueous phase outlet 11 in the form of droplets of each tubing
- the aqueous phase injection is advantageously carried out by an aqueous phase outlet orifice in the form of a slot or plane sprayer, using a nozzle. (not shown)
- a pressurizing means 12 makes it possible to give the desired pressure to the incoming water via the water supply 8.
- the pressure of the aqueous phase feed 8 is typically between 2 and 150 bar. In a variant, this pressure will rather be between 2 and 20 bar, preferably between 3 and 15 bar and more preferably about 8 bar. In another variant, the pressure will be between 20 and 150 bar, in particular between 30 and 100 bar.
- the mineral compound injection device further comprises a flange 13 provided with through holes 18 for bolting or otherwise securing the flue gas treatment device to a flue gas duct.
- the flue gas duct 3 to be treated comprises an orifice for the introduction of the device 1. It is introduced into this orifice and fixed to the duct in a current manner, by the flange 13 and fixing means 15.
- the clamping of the flange 13 maintains a support on the outer face 16 of the flue gas duct 3, but also ensures the sealing of the connection of the device according to the present invention. invention.
- a second flange 7 is present on the flue gas treatment device.
- This flange 17 is provided with a series of through holes 19 arranged to receive fastening means.
- the flange 17 is arranged to be connected to a current source of mineral compound (not shown).
- an outer envelope 20 is present around said peripheral space 9.
- the outer envelope 20 preferably has a diameter of between 100 and 250 mm, preferably less than 200 mm and more preferably between 10 and 170 mm, in particularly between 125 and 150 mm.
- an insulating layer may be provided between the outer face 4 of said powdery mineral compound injection pipe and the outer shell 20.
- the insulation may be simply air or any material insulation known to those skilled in the art. It avoids the cooling of the outer face 4 which is isolated from the tubing 6 which reduces the risk of agglomeration against the inner face 5 of the mineral compound circulating in the mineral compound injection tubing.
- the device according to the present invention further preferably comprises a cap or closure device 21 of said peripheral space.
- This cap is provided with a series of orifices, among which an outlet orifice for the mineral compound 14 and as many outlet orifices for the aqueous phase 11 as there are aqueous phase tubes 6 present.
- the device according to the present invention comprises such a cylindrical mineral compound injection tube 2 which has been modified in such a way that at least one aqueous phase injection tubing 6 can be inserted along the length of the substantially cylindrical tube.
- FIGS. 1A, 1B and 3 eight injection tubings of aqueous phase 6, in the form of droplets, have been placed around the mineral compound injection pipe 2, and the diameters of these tubing 6 were chosen so that the tubing 6 can integrate into the flange 13.
- the powdery inorganic compound injection tubing 2 has a diameter of between 75 and 150 mm, preferably between 80 and 125 mm and in particular about 100 mm.
- each water injection tubing 6 has a diameter of between 5 and 30 mm, preferably between 6 and 20 mm and more preferably between 8 and 16 mm.
- the device according to the present invention When it is desirable to treat flue gas in a pipe with hydrated lime to cut acid pollutants among others, the device according to the present invention is positioned as illustrated for example in FIG. 3. Hydrated lime is then injected into the hydrated lime injection tubing 2 and leaves the tubing via the outlet orifice 14. At this moment, a cloud of hydrated lime, the particles of which typically have an average particle size d 50 of less than 80 ⁇ , advantageously less than 50 ⁇ , preferably less than 35 ⁇ m, preferably less than 25 ⁇ and in particular less than or equal to 0 ⁇ m, in particular less than or equal to 8 ⁇ m, is formed in the flue gas line to be treated. 3.
- the hydrated lime before injection into the flue gases, has a moisture content of between 0.2 and 10% by weight, in particular between 0.5 and 4%. by weight, preferably less than 2%, in particular less than 1.5%.
- the aqueous phase under pressure enters the distributor 7 via said feed 8 and then enters the water injection pipes 6 for which the valves 1 or some of them are in the open position.
- the step of injecting the aqueous phase in the form of droplets is carried out in said cloud or stream of mineral compound in said flue gas pipe 3, in a neighborhood immediately downstream of said point of injection of the mineral compound with respect to the flow direction of the flue gas (indicated by a double arrow G in FIG. 3), and this, in said flue gas duct 3.
- the injected powdery mineral compound is moistened and little or no flue gases to be treated.
- the injection of droplets of aqueous solution into a neighborhood immediately downstream of the injected mineral compound particles, with respect to the direction of flow of the flue gas to be treated, is carried out in this embodiment by closing the valves 10 present on the water phase injection pipes 6 located upstream and opening those of downstream pipes.
- only the pressurized aqueous phase droplet injection pipes situated in the part S of the flue gas treatment device according to the present invention may have their valves in the open position while the other pressurized droplet injection manifolds have valves in the closed position.
- the injected aqueous phase droplets are introduced into a neighborhood immediately downstream of the point of injection of mineral compound particles, and the mineral compound particles are advantageously moistened.
- the pollutants of the flue gases are then captured by said mineral compound and this in an improved manner by the presence of the particles of aqueous phase surrounding the particles of inorganic compound. Then, the mineral compound enriched in pollutant compounds and pollutant-depleted flue gases are recovered separately in the usual manner, in particular by filtration.
- the mixed device for injecting mineral compound / aqueous phase according to the present invention is therefore a simple, easy and inexpensive concept that improves the capture of acid gases from flue gas.
- the temperature of the flue gases is typically between 100 and 1100 ° C. In some installations, this temperature varies from 110 ° C. to 350 ° C., preferably from 130 ° C. to 250 ° C., and more preferably from 150 ° C. to 230 ° C., in particular 180 ° C. to 220 ° C.
- the temperature of the flue gases is typically between 250 ° C and 500 ° C or between 850 and 1100 ° C further upstream ⁇ closer to the zone combustion), preferably between 300 ° C and 450 ° C or between 900 and 1100 ° C further upstream and preferably between 330 ° C and 400 ° C or between 950 ° C and 1050 D C further upstream.
- the effect of the humidification of the mineral compound is of relatively short duration since the droplets of aqueous phase evaporate very quickly in the hot gases. Therefore, the contact between the mineral compound particles injected into the flue gases and the water droplets must be obtained as quickly as possible.
- the size of the aqueous phase droplets is on average between 500 and 5000 ⁇ m, preferably between 500 and 1000 ⁇ m, or between 1000 and 5000 ⁇ m depending on the injection conditions, and is obtained in particular by using nozzle ports.
- Flat outlet in the form of slits through which the aqueous phase droplets are formed.
- the size of the droplets obtained also promotes the contact between the droplets of aqueous phase injected into the cloud of mineral compound particles and the mineral compound particles as soon as they are injected into the flue gas duct.
- a mineral composition in particular a moist hydrated lime (containing more than 2% or even 4% water) or previously moistened because of the agglomeration of the particles. which occurs and clogs the injection tubing.
- a hydrated moist or previously moistened lime is more easily subject to carbonation (fairly fast), which induces a reduction of the capture performance.
- agglomerated particles of mineral compound, in particular hydrated hydrated lime have reduced capture capacities because of the decrease in accessibility to their pores. Typically, it is the fine particles that are sought to improve the capture performance.
- the use of the device according to the present invention allows the fine particles of mineral compound injected into the flue gas line to be treated to be wetted as such, in situ, and react with the particular acidic gases in the cloud of droplets. water phase created directly and also dry in situ because the evaporation is very fast in the hot flue gases. As a result, evaporation of water occurs before the particles have time to agglomerate.
- the amount of water injected is only the amount of water needed to humidify the mineral compound particles and to create a cloud formed of mineral compound particles and phase droplets.
- aqueous aqueous.
- the weight ratio between the said injected aqueous phase in the form of droplets and the said injected powdery mineral compound is less than or equal to 1, 2, preferably less than or equal to 1 and in particular less than or equal to 0.8.
- the aforementioned weight ratio is also greater than or equal to 0.1 and particularly greater than or equal to 0.2. Consequently, the aqueous phase injected in the form of fine droplets has little impact on the temperature of the flue gas to be treated and does not disturb the subsequent potential stages of heat recovery.
- the flue gases have, after injection of the mineral compound and of the aqueous phase in the form of droplets, a temperature of between n and n-0 ° C., preferably between n and n-8 ° C., preferably between n and n - 5 ° C, in particular n - 3 ° C, n being the temperature of the flue gases before injection of the inorganic compound and of said aqueous phase.
- the two aqueous phase and mineral compound injection systems are typically attached to the same flue gas treatment device, it goes without saying that they operate independently of one another. . As a result, it is possible to work only by injecting droplets of aqueous phase or only the mineral compound, if the case requires it.
- Figure 2 illustrates a variant of the flue gas treatment device according to the present invention.
- the device 1 here comprises a powdery mineral compound injection tubing 2 connected to a source of powdery mineral compound (not shown).
- the mineral compound injection tubing is arranged to open into said flue gas duct 3 (see FIGS. 4 and 5) and to allow the mineral compound to exit via an inorganic compound outlet orifice 14.
- the injection manifold of mineral compound 2 has an outer face 4 and an inner face 5. In operation, the inner face 5 is in contact with said powder mineral compound which is injected into the injection pipe 2.
- the pulverulent inorganic compound injection device 1 also comprises an aqueous phase injection pipe 6 in the form of droplets, which is connected to an aqueous phase feed 8, and which is located in a concentric tube located in the space 9.
- the aqueous phase injection tubing although not shown here, may further include a stop valve 10.
- the aqueous phase outlet port 11 in the form of droplets of the tubing.
- Aqueous phase injection is in practice carried out in the form of a slot or a planar sprayer.
- the pressure of the aqueous phase feed 8 is typically between 2 and 150 bar. In a variant, this pressure will rather be between 2 and 20 bar, preferably between 3 and 5 bar and more preferably about 8 bar. In an other alternatively, the pressure will be between 10 and 150 bar, in particular between 20 and 100 bar. These high pressures make it possible to prevent fouling of the spray pipe.
- the mineral compound injection device further comprises a flange 13 provided with through openings 18 for bolting or otherwise securing the flue gas treatment device to a flue gas duct via a flange 23.
- the flue gas duct 3 to be treated may comprise an introduction duct 22 for the device 1 according to the present invention.
- the introduction duct 22 is provided with a flange 23 at its end.
- the device according to the present invention 1 is introduced into this duct and fixed on it with the aid of the flanges 13 and 23.
- the step of injecting the powdery mineral compound is carried out in the flue gas duct 3 at an angle of 90 to 150 degrees, preferably less than or equal to 145 degrees, preferably less than or equal to 140 degrees and in particular less than or equal to 135 degrees, with respect to the flow direction G of the flue gases.
- This orientation of the tubular of the mineral compound with respect to the flow direction of the flue gases is in no way related to the embodiment of the device according to the invention.
- the embodiment comprising a plurality of aqueous phase injection tubing shown in FIGS. 1 and 3 may also be inclined with respect to the wall of the flue gas duct.
- the device according to the present invention in the version illustrated in FIGS. 1A, 1B, 2A and 2B, may be more or less inserted in the flue gas duct, depending on the desideratas and may typically penetrate a length between 0 and 40 cm in the gas line.
- Technical considerations such as tubing length, operating parameters of the device according to the present invention, in this embodiment, vary in the same way as described for FIGS. 1A, 1B and 3.
- a second flange 17 is present on the flue gas treatment device.
- This flange 17 is provided with a series of through holes 19 arranged to receive a fixing means.
- the flange 17 is arranged to be connected to a source of mineral compound (not shown).
- an outer envelope 20 is present around said peripheral space 9.
- the outer envelope 20 preferably has a diameter of between 100 and 250 mm, preferably less than 200 mm and more preferably between 110 and 170 mm, in particular between 125 and 50 mm.
- an insulating layer may be provided between said outer face 4 of said powdery inorganic compound injection tubing and the outer shell 20.
- the insulation may be simply air or any insulator known to those skilled in the art and makes it possible to avoid the cooling of the outer face 4, thus isolated from the aqueous solution tubing 6, which reduces the risks of agglomeration of the particles of the mineral compound, in particular hydrated lime, circulating in the injection pipe 2.
- the device according to the present invention further preferably comprises a cap or closure device 21 of said peripheral space provided with a series of orifices among which a mineral compound outlet orifice 14 and an outlet port of the tube concentric with the tubing of aqueous phase injection 11.
- the aqueous phase injection tubing 6 is arranged in a concentric tube, from which the aqueous phase injection tubing 25 is retractable. , which allows clean or change the injection tubing of the aqueous phase without stopping the injection of mineral compound.
- the present invention provides a slight curvature in the mineral compound injection tubing, which remains as small as possible to avoid obstacles within the essentially cylindrical tube of supply of mineral compound 2 and thus reduce the agglomeration of mineral compound on the walls.
- the main mineral compound injection pipe typically has a diameter of 100 mm and the concentric tube with the aqueous phase injection pipe has a diameter of 25 mm. mm. Both tubes are confined in an envelope 20 having a diameter of about 125 mm.
- the first sample (Ech 1) was a hydrated lime obtained according to the teaching of the patent application WO 97/14650.
- the second sample (Ech 2) was a hydrated lime obtained according to the teaching of the patent application WO 2007/000433.
- the table shows the SO 2 abatement rates obtained by varying the humidity of the reagents tested by 0.7% by weight relative to the weight of hydrated lime at 4.1% by weight, for a stoichiometric factor of 2, 5 and a flow rate of Q absorbent.
- the flow rate of absorbent Q corresponds to the flow of hydrated lime necessary for the neutralization of the flow rate of S0 2 , if the yield of the reaction was 100% (stoichiometric equilibrium), multiplied by a "stoichiometric" factor, taking into account that part of the injected absorbent does not actually participate in the reaction.
- Q is 5.05 g / h.
- the parameters of the flue gas are as follows:
- a hydrated lime prepared according to the teaching of the patent application WO2007 / 000433 was injected upstream of a filter to sleeves for the reduction of S0 2 .
- S0 2 content 1800 mg / Nm 3 upstream of the bag filter and 700 mg / Nm 3 at the outlet
- a reduction of 15 to 20% in the consumption of lime was observed when the lime was moistened with water.
- comparison of the situation when the lime was not humidified (17 dm 3 / h water or water / lime weight ratio of 0.25).
- a lime conversion rate of 35% is observed when the lime is not moistened and 40% when it is moistened.
- the device of Figure 1 according to the present invention has been used; it had an inclination of about 120 ° with respect to the direction of gas flow.
- the parameters of the flue gas are as follows:
- a hydrated lime prepared according to the teaching of the patent application WO 2007/000433 was injected upstream of a bag filter to study the effects of its humidification rate on the S0 2 abatement rates.
- an SO 2 content at the filter outlet of respectively 134 mg / Nm 3 (equivalent to a lime conversion rate of 53%) when the lime is not moistened and 1 12 mg / Nm 3 (lime conversion rate of 67%) when the lime is moistened at a rate of 30 dm 3 / h of water (weight ratio water / lime 0.6). It is therefore observed that the moistened lime allows a reduction of SO 2 of 25% in comparison with the same non-moistened lime.
- a standard hydrated lime was injected into the same plant and with the same flue gas parameters as the example 3 to study the effects of its rate of moistening the S0 2 abatement rate.
- an SO 2 content at the outlet of the filter of respectively 336 mg / Nm 3 (equivalent to a lime conversion rate of 20%) when lime is not moistened, 266 mg / Nm 3 (lime conversion rate of 37%) when lime is moistened at a rate of 30 dm 3 / h of water (water / lime weight ratio of 0.25) and 241 mg / Nm 3 (lime conversion rate of 43%) when the lime is moistened at the rate of 20 dm 3 / h of water (water / lime mass ratio of 1). It is therefore observed that a lime moistened with 30 and 120 dm 3 / h of water allows a reduction of S0 2 reduction of respectively 85% and 10% in comparison with the same unhumidified lime.
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Abstract
Description
Claims
Priority Applications (1)
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PL14736324T PL3013459T3 (pl) | 2013-06-25 | 2014-06-20 | Sposób i urządzenie do obróbki gazu przez wtryskiwanie związku w postaci proszku i fazy wodnej |
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BE20130435A BE1021596B9 (fr) | 2013-06-25 | 2013-06-25 | Procede et dispositif de traitement de gaz par injection de compose pulverulent. |
PCT/EP2014/063017 WO2014206880A1 (fr) | 2013-06-25 | 2014-06-20 | Procede et dispositif de traitement de gaz par injection de compose pulverulent et de phase aqueuse |
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EP3013459A1 true EP3013459A1 (fr) | 2016-05-04 |
EP3013459B1 EP3013459B1 (fr) | 2017-01-11 |
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EP14736324.6A Active EP3013459B1 (fr) | 2013-06-25 | 2014-06-20 | Procede et dispositif de traitement de gaz par injection de compose pulverulent et de phase aqueuse |
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US (1) | US9579601B2 (fr) |
EP (1) | EP3013459B1 (fr) |
JP (1) | JP6059828B2 (fr) |
AU (1) | AU2014301338B2 (fr) |
BE (1) | BE1021596B9 (fr) |
BR (1) | BR112015030657B1 (fr) |
CA (1) | CA2913240C (fr) |
CL (1) | CL2015003573A1 (fr) |
DK (1) | DK3013459T3 (fr) |
ES (1) | ES2615804T3 (fr) |
FR (1) | FR3007297A1 (fr) |
MY (1) | MY164819A (fr) |
PL (1) | PL3013459T3 (fr) |
PT (1) | PT3013459T (fr) |
SG (1) | SG11201510356TA (fr) |
WO (1) | WO2014206880A1 (fr) |
ZA (1) | ZA201509110B (fr) |
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WO2020208000A1 (fr) * | 2019-04-09 | 2020-10-15 | S.A. Lhoist Recherche Et Developpement | Dispositif et procédé pour disperser des particules de sorbant dans un conduit de gaz de combustion |
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US7827032B2 (en) | 2005-02-04 | 2010-11-02 | Vocollect, Inc. | Methods and systems for adapting a model for a speech recognition system |
US8914290B2 (en) | 2011-05-20 | 2014-12-16 | Vocollect, Inc. | Systems and methods for dynamically improving user intelligibility of synthesized speech in a work environment |
US9978395B2 (en) | 2013-03-15 | 2018-05-22 | Vocollect, Inc. | Method and system for mitigating delay in receiving audio stream during production of sound from audio stream |
WO2018095553A1 (fr) | 2016-11-28 | 2018-05-31 | S.A. Lhoist Recherche Et Developpement | Procédé de transport pneumatique d'un matériau pulvérulent |
TW201825375A (zh) | 2016-11-28 | 2018-07-16 | 比利時商耐斯赤理查發展公司 | 氣動傳送粉狀材料之方法 |
CN108392946A (zh) * | 2018-04-13 | 2018-08-14 | 河南科技大学第附属医院 | 一种双极电凝钳的烟气净化处理装置 |
CN110102171A (zh) * | 2019-04-26 | 2019-08-09 | 核工业北京化工冶金研究院 | 一种锂云母矿预处理尾气吸收装置及方法 |
CN112696680A (zh) * | 2020-12-26 | 2021-04-23 | 浙江大学 | 利用磷基耦合碱性材料抑制固废焚烧生成二噁英的方法 |
CN113385027A (zh) * | 2021-08-17 | 2021-09-14 | 佛山赛因迪环保科技有限公司 | 一种脱硫剂及其制备方法和应用 |
CN115624862B (zh) * | 2022-10-13 | 2023-08-18 | 大唐长春第三热电厂 | 一种自动化喷氨格栅 |
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WO2020208000A1 (fr) * | 2019-04-09 | 2020-10-15 | S.A. Lhoist Recherche Et Developpement | Dispositif et procédé pour disperser des particules de sorbant dans un conduit de gaz de combustion |
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JP6059828B2 (ja) | 2017-01-11 |
AU2014301338B2 (en) | 2016-08-25 |
CA2913240A1 (fr) | 2014-12-31 |
JP2016530981A (ja) | 2016-10-06 |
US20160129394A1 (en) | 2016-05-12 |
BE1021596B9 (fr) | 2018-06-18 |
EP3013459B1 (fr) | 2017-01-11 |
BE1021596B1 (fr) | 2015-12-17 |
WO2014206880A1 (fr) | 2014-12-31 |
AU2014301338A1 (en) | 2015-12-24 |
DK3013459T3 (en) | 2017-02-27 |
ES2615804T3 (es) | 2017-08-25 |
ZA201509110B (en) | 2017-11-29 |
PT3013459T (pt) | 2017-02-17 |
CA2913240C (fr) | 2016-11-22 |
CL2015003573A1 (es) | 2016-07-15 |
BR112015030657B1 (pt) | 2021-08-31 |
SG11201510356TA (en) | 2016-01-28 |
BR112015030657A2 (pt) | 2017-07-25 |
FR3007297A1 (fr) | 2014-12-26 |
MY164819A (en) | 2018-01-30 |
US9579601B2 (en) | 2017-02-28 |
PL3013459T3 (pl) | 2017-07-31 |
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